chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121241687512416876TC25GENIChomozygous115416400
121241955612419557CT28GENIChomozygous115258393
121242129812421299GA26GENIChomozygous115416402
121242262912422630GA28GENIChomozygous115258397
121242361012423611TC21GENIChomozygous115258399
121242392312423924CA21GENIChomozygous115258401
121242433612424337AG16GENIChomozygous115258403
121242545712425458GA23GENIChomozygous115258405
121242885412428855CA35GENIChomozygous115361997
121242885512428856AC35GENIChomozygous115361998
121242889912428900AC34GENIChomozygous115361999
121243294512432946CA19GENIChomozygous115258421
121243398612433987CG25GENIChomozygous115416404
121243399312433994TC26GENIChomozygous115416406
121243567412435675CT37GENIChomozygous115416408
121243763512437636AG21GENIChomozygous115416410
121244087212440873AT20GENIChomozygous115416412
121244285312442854GA22GENIChomozygous115362004
121244779512447796AC37GENIChomozygous115416414
121244804012448041TC23GENIChomozygous115258431
121244830812448309TC33GENIChomozygous115258433
121245025312450254AC26GENICheterozygous115505100
121245218312452184TC27GENIChomozygous115258441
121245719712457198AT18GENIChomozygous115416416
121245791712457918AG17GENIChomozygous115416418
121245796112457962AG19GENIChomozygous115258453
121245802112458022TC20GENIChomozygous115258455
121245864412458645GA21GENIChomozygous115416420
121246306212463063AG24GENIChomozygous115258467
121246510112465102TC23GENIChomozygous115258469
121246540612465407AG31GENIChomozygous115258471
121246553612465537CA36GENIChomozygous115416422
121246558112465582CG27GENIChomozygous115416424
121246558812465589CA29GENIChomozygous115416426
121252751912527520GC29GENIChomozygous115362010
121252753012527531CT30GENIChomozygous115416428
121252778612527787CT20GENIChomozygous115362011
121252781512527816GA29GENIChomozygous115362012
121252828412528285TC33GENIChomozygous115258479
121254462412544625TC30GENIChomozygous115258503